Dual roles of UPRer and UPRmt in neurodegenerative diseases
Author:
Funder
National Natural Science Foundation of China
Natural Science Foundation of Liaoning Province
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Drug Discovery,Molecular Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00109-023-02382-9.pdf
Reference79 articles.
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2. Fiorese CJ, Haynes CM (2017) Integrating the UPR(mt) into the mitochondrial maintenance network. Crit Rev Biochem Mol Biol 52(3):304–313. https://doi.org/10.1080/10409238.2017.1291577
3. Dugger BN, Dickson DW (2017) Pathology of neurodegenerative diseases. Cold Spring Harb Perspect Biol 9(7). https://doi.org/10.1101/cshperspect.a028035
4. Vincenz-Donnelly L, Hipp MS (2017) The endoplasmic reticulum: a hub of protein quality control in health and disease. Free Radical Biol Med 108:383–393. https://doi.org/10.1016/j.freeradbiomed.2017.03.031
5. Fregno I, Molinari M (2019) Proteasomal and lysosomal clearance of faulty secretory proteins: ER-associated degradation (ERAD) and ER-to-lysosome-associated degradation (ERLAD) pathways. Crit Rev Biochem Mol Biol 54(2):153–163. https://doi.org/10.1080/10409238.2019.1610351
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